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rs206468

From SNPedia

Orientationminus
Stabilizedminus
Make rs206468(A;A)
Make rs206468(A;G)
Make rs206468(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position10296941
is asnp
is mentioned by
dbSNPrs206468
dbSNP (classic)rs206468
ClinGenrs206468
ebirs206468
HLIrs206468
Exacrs206468
Gnomadrs206468
Varsomers206468
LitVarrs206468
Maprs206468
PheGenIrs206468
Biobankrs206468
1000 genomesrs206468
hgdprs206468
ensemblrs206468
geneviewrs206468
scholarrs206468
googlers206468
pharmgkbrs206468
gwascentralrs206468
openSNPrs206468
23andMers206468
SNPshotrs206468
SNPdbers206468
MSV3drs206468
GWAS Ctlgrs206468
GMAF0.3338
Max Magnitude0
GWAS
SNP rs11209003,rs11209002,rs206468
PubMedID [PMID 17804789OA-icon.png]
Condition Crohn's disease
Gene IL23R
Risk Allele
pValue 2.00E-007
OR 2.56
95% CI 1.75-3.70